A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5546208



Internal ID320183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:39165396..39165446hg38UCSC Ensembl
chr11:39186946..39186996hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043804
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5546208
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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